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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Cancer Urology</journal-id><journal-title-group><journal-title xml:lang="en">Cancer Urology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкоурология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9776</issn><issn publication-format="electronic">1996-1812</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">496</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>CLINICAL CASE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>КЛИНИЧЕСКИЙ СЛУЧАЙ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="ru">Опыт применения сунитиниба при метастатическом почечно-клеточном раке в Центральной и Восточной Европе: субанализ международного исследования расширенного доступа</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Vrdoljak</surname><given-names>Eduard</given-names></name><address><country country="RU">Russian Federation</country></address><email>edo.vrdoljak@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Géczi</surname><given-names>Lajos</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Mardiak</surname><given-names>Jozef</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Ciuleanu</surname><given-names>Tudor-Eliade</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Leyman</surname><given-names>Sophie</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>Zhang</surname><given-names>Ke</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Sajben</surname><given-names>Peter</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff7"/></contrib><contrib contrib-type="author"><name><surname>Torday</surname><given-names>Laszlo</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff8"/></contrib></contrib-group><aff id="aff1"><institution>Medical School Split, Center of Oncology, University Hospital Split, Spinciceva 1, 21 000 Split, Croatia</institution></aff><aff id="aff2"><institution>National Institute of Oncology, Budapest, Hungary</institution></aff><aff id="aff3"><institution>Department of Medical Oncology, National Cancer Institute, Bratislava, Slovak Republic</institution></aff><aff id="aff4"><institution>Institute of Oncology Ion Chiricuta, University of Medicine and Pharmacy Iuliu Hatieganu, Cluj-Napoca, Romania</institution></aff><aff id="aff5"><institution>Pfizer Inc., Brussels, Belgium</institution></aff><aff id="aff6"><institution>Pfizer Inc., La Jolla, CA, USA</institution></aff><aff id="aff7"><institution>Pfizer Inc., New York, NY, USA</institution></aff><aff id="aff8"><institution>Department of Oncotherapy, University of Szeged, Szeged, Hungary</institution></aff><pub-date date-type="pub" iso-8601-date="2015-09-30" publication-format="electronic"><day>30</day><month>09</month><year>2015</year></pub-date><volume>11</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>101</fpage><lpage>107</lpage><history><date date-type="received" iso-8601-date="2015-09-24"><day>24</day><month>09</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-09-24"><day>24</day><month>09</month><year>2015</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncourology.abvpress.ru/oncur/article/view/496">https://oncourology.abvpress.ru/oncur/article/view/496</self-uri><abstract xml:lang="ru"><p>Международное открытое исследование расширенного доступа предусматривало лечение сунитинибом пациентов с метастатическим почечно-клеточным раком (мПКР) в период с 2005 по 2011 г. в рамках программы благотворительно-исследовательского применения. В данном ретроспективном анализе оценены исходы терапии у пациентов из стран Центральной и Восточной Европы (ЦВЕ), участвующих в международном открытом исследовании расширенного доступа. Сунитиниб (начальная доза 50 мг 1 раз в день перорально, со снижением дозы в случае развития токсичности) назначался в виде повторных 6-недельных циклов (4 нед лечения и 2 нед перерыв) до прогрессирования заболевания или развития неприемлемой токсичности. Оценку опухолевых очагов выполняли на основании критериев RECIST (Критерии оценки ответа при солидных опухолях) в соответствии с местными стандартами лечения. В общей сложности 401 пациент стран ЦВЕ получил лечение сунитинибом (медиана длительности лечения 9,6 мес), из которых у 378 оценивали ответ опухоли на терапию. Наиболее частыми нежелательными явлениями III степени тяжести и выше были утомляемость (7,5 %), артериальная гипертензия (7,0 %), тромбоцитопения (6,5 %), диарея (4,2 %), тошнота (3,7 %), ладонно-подошвенный синдром (3,7 %) и нейтропения (3,0 %). Медиана общей выживаемости составила 30,7 мес (95 % доверительный интервал (ДИ) 23,3– … мес). Общая выживаемость, как правило, была выше у пациентов без предшествующей терапии цитокинами по сравнению с пациентами, получавшими цитокины в первой линии (медиана 60,8 мес против 27,5 мес; p = 0,1324). Среди пациентов, у которых оценивали ответ опухоли на терапию, 4,0 % достигли полного и 14,6 % частичного ответа (частота объективного ответа 18,5 % (95 % ДИ 14,7–22,8)). Медиана выживаемости без прогрессирования составила 11,6 мес (95 % ДИ 10,3–12,8). В условиях релаьной клинической практики Сунитиниб продемонстрировал эффективность и безопасность у больных мПКР в странах ЦВЕ. В рамках программы расширенного доступа регистрировалась более низкая частота ответа опухоли на терапию, однако результаты выживаемости были сопоставимы с данными показателями, полученными для сунитиниба в клиническом исследовании III фазы при мПКР.</p></abstract><kwd-group xml:lang="ru"><kwd>почечно-клеточный рак</kwd><kwd>метастатический рак</kwd><kwd>сунитиниб</kwd><kwd>исследование расширенного доступа</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Mena A.C., Pulido E.G., Guillén-Ponce C. Understanding the molecular-based mechanism of action of the tyrosine kinase inhibitor: sunitinib. Anti-Cancer Drugs 21 Suppl. 1: S3-S11. doi: 10.1097/01.cad.0000361534.44052.c5.</mixed-citation><mixed-citation xml:lang="ru">Mena A.C., Pulido E.G., Guillén-Ponce C. Understanding the molecular-based mechanism of action of the tyrosine kinase inhibitor: sunitinib. 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